Canonical Allele Identifier: CA101489374
Gene:

Linked Data

dbSNP Id: rs552243819
gnomAD v2: 4-90577169-G-T
gnomAD v3: 4-89656018-G-T
gnomAD v4: 4-89656018-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89656018G>T , CM000666.2:g.89656018G>T GRCh38
NC_000004.11:g.90577169G>T , CM000666.1:g.90577169G>T GRCh37
NC_000004.10:g.90796192G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+28101G>T
XR_938987.1:n.688+28101G>T
XR_938988.1:n.554+28101G>T
XR_938990.1:n.299-35267G>T
XR_938991.1:n.434+28101G>T
XR_938994.1:n.779+28101G>T
XR_938995.1:n.613+28101G>T
XR_938986.2:n.459+28101G>T
XR_938987.2:n.748+28101G>T